EP2390344A1 - Film de cellulose bactérienne et utilisations associées - Google Patents

Film de cellulose bactérienne et utilisations associées Download PDF

Info

Publication number
EP2390344A1
EP2390344A1 EP11167341A EP11167341A EP2390344A1 EP 2390344 A1 EP2390344 A1 EP 2390344A1 EP 11167341 A EP11167341 A EP 11167341A EP 11167341 A EP11167341 A EP 11167341A EP 2390344 A1 EP2390344 A1 EP 2390344A1
Authority
EP
European Patent Office
Prior art keywords
bacterial cellulose
cellulose film
film
skin
bacterial
Prior art date
Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
Granted
Application number
EP11167341A
Other languages
German (de)
English (en)
Other versions
EP2390344B1 (fr
Inventor
Yi-Chuan LIN
Yuh-Chyun WEY
Mei-Ling Lee
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
NYMPHEAS INTERNATIONAL CORPORATION
Original Assignee
NYMPHEAS INTERNATIONAL BIOMATERIAL CORP
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Application filed by NYMPHEAS INTERNATIONAL BIOMATERIAL CORP filed Critical NYMPHEAS INTERNATIONAL BIOMATERIAL CORP
Publication of EP2390344A1 publication Critical patent/EP2390344A1/fr
Application granted granted Critical
Publication of EP2390344B1 publication Critical patent/EP2390344B1/fr
Not-in-force legal-status Critical Current
Anticipated expiration legal-status Critical

Links

Images

Classifications

    • CCHEMISTRY; METALLURGY
    • C12BIOCHEMISTRY; BEER; SPIRITS; WINE; VINEGAR; MICROBIOLOGY; ENZYMOLOGY; MUTATION OR GENETIC ENGINEERING
    • C12PFERMENTATION OR ENZYME-USING PROCESSES TO SYNTHESISE A DESIRED CHEMICAL COMPOUND OR COMPOSITION OR TO SEPARATE OPTICAL ISOMERS FROM A RACEMIC MIXTURE
    • C12P19/00Preparation of compounds containing saccharide radicals
    • C12P19/04Polysaccharides, i.e. compounds containing more than five saccharide radicals attached to each other by glycosidic bonds
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P17/00Drugs for dermatological disorders

Definitions

  • the present invention relates to a bacterial cellulose film, and in particular relates to a bacterial cellulose film with a density gradient in the direction of the film thickness.
  • Bacterial cellulose also named microbial cellulose, refers to cellulose produced by microorganisms. Bacterial cellulose is formed by a linkage of ⁇ -1,4 glucosidic bonds between carbon atoms and shows properties of high purity and water content, and excellent ductility and mechanical strength.
  • the strain for producing bacterial cellulose includes Acetobacter xylinum.
  • the obtained cellulose generally forms fibers which constitute a non-woven film in a reticular structure on the surface of a culture medium.
  • the fiber in general has a diameter of approximately 2 ⁇ 100nm, which is about 1/100th fiber diameter of the plant.
  • the fiber of bacterial cellulose has a chemical structure identical to the plant fiber.
  • bacterial cellulose is applicable in several fields, such as biomedical materials (EP 1,438,975 , EP 0,396,344 or WO 01-61026 ), electronic materials ( US 2008/220333 ), acoustics ( EP 0,457,474 , US 5,274,199 or JP 6-284495 ) and special papers and cosmetics ( JP 10-077302 , JP9-838803 or FR 2,924,342 ) etc.
  • the bacterial cellulose film has been considered one of the best substitutes for skin, providing effects of alleviating pain, absorbing secretions from wounds, providing wounds with water and enhancing and improving the wound recovery.
  • the bacterial cellulose film also shows excellent biocompatibility and biosafety.
  • WO 86/02095 discloses a method for producing a bacterial cellulose film with a thickness of about 0.2-3mm by culturing A. xylinum in a medium containing Tea Sinesis as nitrogen sources and glucose as carbohydrate sources under 26 ⁇ 96 hours of stirring at a temperature of 28°C. A film produced by the method has been sold as a trademark BIOFILL® for treatment of skin injuries like artificial skin substitutes.
  • US 2005/0019380A1 provides a use for bacterial cellulose film to treat chronic wounds.
  • WO2005/018435A2 and US2007/0286884A1 discloses an implantable microbial cellulose material for hard tissue repair and regeneration.
  • EP1849463A2 provides a microbial cellulose material for use in transdermal drug delivery systems.
  • FR 2924340 discloses a use of fingers maintenance and cosmetics.
  • FR2924342 provides a use for lip care and cosmetics.
  • JP2009-051829 discloses a combination of microbial cellulose films and cosmetic powders.
  • FR2916948 discloses a long-lasting perfume primarily constituted of microbial cellulose films.
  • FR2916971 provides a microbial cellulose paste for puffy eyes.
  • the bacterial cellulose film has been prospected for broad uses. Study for new applications and novel properties of the bacterial cellulose film are already flourishing in the field.
  • the invention provides a bacterial cellulose film that comprises microbial fibers consisting of bacterial cellulose, in which the microbial fibers are arranged in a density gradient in a direction of the bacterial cellulose film thickness.
  • the invention provides a method, for producing the bacterial cellulose film, comprises a fermentation step with a low initial cell concentration in the range of 10 2 -10 5 /ml.
  • the invention provides a method for using the bacterial cellulose film by applying the bacterial cellulose film onto a skin surface, wherein the surface of the bacterial cellulose film in contact with the skin surface has a lower density of microbial fibers than the other surface of the bacterial cellulose film.
  • the invention provides a method for removing sebum from the skin surface by applying the bacterial cellulose film onto the skin surface, wherein the surface of the bacterial cellulose film in contact with the skin surface has a lower density of microbial fibers than the other surface of the bacterial cellulose film.
  • the bacterial cellulose film consists of cellulose produced by culturing the bacteria, Gluconacetobacter xylinum , in a liquid medium.
  • the diameter of microbial fibers for bacterial cellulose films is about 30 ⁇ 100nm. After static fermentation, the microbial fibers constitute a non-woven reticular structure on the surface of the culture medium and form a semi-transparent bacterial cellulose film. In the embodiment, one bacterial cellulose film is produced at one time.
  • the formation of bacterial cellulose film with a density gradient of microbial fibers in a direction of the bacterial cellulose film thickness can be achieved by manipulating inoculates concentration and culture conditions.
  • the dissolution of oxygen in the medium is critical for cell growth and biocellulose formation.
  • the formation biocellulose films are happened at the air/liquid medium interface for static cultures.
  • low cell concentration and/or low cell growth rate can result in loose and softer microbial fibers.
  • the amount of bacteria increases and/or culture conditions are changed to speed up biocellulose formation.
  • the reticular structure of biocellulose becomes tight and the density of the microbial fibers increases.
  • bacterial cellulose films are formed at the air/liquid medium interface, the new cellulose is formed at the top of existing cellulose.
  • the formation of bacterial cellulose film is from the top down so that each bacterial cellulose film in the medium has an upper surface contacting with the air and formed by later produced cellulose.
  • the other surface of the bacterial cellulose film, the lower surface, is close to the bottom of the medium.
  • the bacterial cellulose film according to the invention has an upper surface shows a tight reticular structure and has higher density of microbial fibers.
  • the other surface of the bacterial cellulose film, the lower surface is close to the bottom of the medium.
  • the lower surface consisting of earlier produced celluloses and the reticular structure is more loose and softer. As such, the lower surface has a lower density of microbial fibers than the upper surface.
  • the difference between the upper and lower surface of the bacterial cellulose film can be observed under a scanning electron microscope (SEM). According to the cross section view in a direction of the film thickness, the upper surface shows a more dense structure while the lower surface shows several exposed microbial fibers ( Fig. 1B ). The difference can also be sensed by hand touch.
  • the lower surface is smoother than the upper surface. In other words, the bacterial cellulose film shows a density gradient in the direction of the film thickness and the density decreases gradually from the upper surface to the lower surface when the film is formed in the medium.
  • the bacterial cellulose film of the present invention can be obtained from an incubation of microorganisms.
  • the microorganism comprises bacteria or fungi capable of producing celluloses. More specifically, the microorganism includes Glyconacetobacter , and Glyconacetobacter xylinum is preferable.
  • the method, for producing the bacterial cellulose film comprises a fermentation step with a low initial cell concentration in the range of 10 2 -10 5 /ml. Specifically, a low initial cell number of Glyconacetobacter in a suitable medium at the beginning of the culture. The low number of the microorganism comprises 10 2 -10 5 cells/ml.
  • the medium consists of glucose, yeast extract powders, Na 2 HPO 4 and citrate acid.
  • the components of the media can be adjusted depending on the species of the cultured microorganism and the characteristics thereof following the culture techniques in the art.
  • the fermentation herein includes a two-step culture condition in addition to the known culture conditions, for slowing down the formation of the cellulose in the beginning of cultivation and following the high speed cellulose formation condition for a cellulose-producing microorganism.
  • the two-step culture condition comprises a two-step culture temperature in which the first step is incubated under room temperature and the second step is incubated under a temperature higher than room temperature. More specifically, the first step is under 25 ⁇ 28°C and the second step is under 29 ⁇ 30°C.
  • the two-step incubation is static in one embodiment. However, the two-step culture condition may be appropriately altered depending on the desired film thickness, the water content, or the like.
  • the "direction of the film thickness” and “direction of the bacterial cellulose film thickness” refer to a direction that the microbial fiber accumulates to form a thickness during the production of the bacterial cellulose film.
  • the direction of the thickness is vertical to the surface of the film.
  • the "density gradient” refers to a density change that gradually increases or decreases from one surface to another of the bacterial cellulose film. For example, when the bacterial cellulose film is formed in the medium and not moved, the cellulose density gradually decreases in a direction from the upper surface (away from the medium plate) to the lower surface (close to the medium plate).
  • microbial cellulose has been developed in China and South-East Asia by conventional methods.
  • the conventional microbial cellulose is produced by artificially incubating mixed cultures in an open environment to form a bulk of cellulose.
  • the bulk of cellulose is then sliced to obtain a cellulose sheet. Therefore, both surfaces of the cellulose sheet show identical density of the cellulose.
  • the cellulose sheet lacks a density gradient in the direction of the thickness.
  • slicing makes the cellulose sheet thicker and heavier than the film produced by culturing bacteria in sheets. As such, when in contact with human or animal skin, the cellulose sheet is unable to closely fit with the surface of skin and easily falls off because it is thick and heavy.
  • microbial cellulose has a property to absorb water or solution more than 50 to 100 times that of its weight. According to the thickness, conventional biocellulose sheets need a lot of essence to rich a state of saturation which is good for active components efficiently delivered into the skin.
  • the bacterial cellulose film according to the invention provides a density gradient in the direction of film thickness.
  • the surface with a lower density of the microbial fibers forms a tight fit to the surface of skin. With the saturation of water content or moisture content, water or active components contained in the film can be efficiently delivered to the skin resulting in effective transdermal delivery.
  • the invention provides a method for using the bacterial cellulose film by applying the film onto the surface of human or animal skin. Specifically, the method makes the surface of the film with a lower density of microbial fibers have contact with the surface of human or animal skin in order to obtain excellent fit for the skin and effective transdermal delivery.
  • skin herein refers to human or animal tissues including epidermis, dermis, subcutaneous tissues, nails, hairs, glands, or the like.
  • the inventors realize that the density gradient in the direction of film thickness leads the bacterial cellulose film to show excellent fitness for the skin when applying the surface with a lower density of the microbial fibers onto human or animal skin.
  • the reason may be that the surface with a lower density of microbial fibers exposes more microbial nano-fibers and form a larger contact area with the skin.
  • the microbial fibers contain a large number of hydroxyl groups (-OH) that easily form hydrogen bonds with the surface of human or animal skin.
  • the bacterial cellulose film is able to nicely fit the skin.
  • the bacterial cellulose film is applied onto the surface of human or animal skin for about 15 to 30 minutes.
  • the bacteria cellulose film is applied on human or animal nails.
  • the bacterial cellulose film is applied on an elbow of a human arm. In this embodiment, even if the arm severely moves, the bacterial cellulose film is still closely fit onto the surface of skin.
  • the bacterial cellulose film is applied on the face like a masque. In the embodiment, the user is free to move and the film does not fall off, decreasing the inconvenience of keeping a fixed head posture when conventionally using masques.
  • the dry weight of the bacterial cellulose film can be controlled by culture conditions, such as culture periods, concentration and volume of the culture medium, or the like. According to the invention, the dry weight of the bacterial cellulose film is controlled in a range of 5 ⁇ 20g/m 2 . Comparing the weight of the conventional cellulose sheet (which is more than 30g/m 2 ), the bacterial cellulose film is at least 33.3% lighter. Because the bacterial cellulose film is softer than conventional ones and is able to be pressed to a thickness of 0.1mm ⁇ 0.5mm, fitness to skin is greatly elevated. The biocellulose film can be easily become saturated after soaked in water or a solution containing active components, because the film is lighter and fibers of each film are less. The saturation of water content in the bacterial cellulose film can enhance the efficiency of the transdermal delivery of water and/or active components
  • the "saturation" in the content refers to a water content of the bacterial cellulose film that is the maxima the bacterial cellulose film can absorb under room temperature and atmospheric pressure.
  • the water content of the bacterial cellulose film according to the invention is 90% ⁇ 99% by weight based on the total weight of the film.
  • the bacterial cellulose film absorbs water only.
  • the bacterial cellulose film contains water and other active components.
  • the active component is not specifically limited, such as antibiotics, antimicrobials, antivirals, hemostatics, anesthetics, anti-inflammatory drugs, drugs for enhancing the healing of wounds, steroids, antihistamine, cell proliferating drugs, growth factors, proteins, nucleotides, enzymes, humectants, hyaluronic acid, ascorbic acid, kojic acid, arbutin, or the like, or a combination thereof.
  • a person skilled in the art can follow the market demand to add appropriate amounts of the active components in the film.
  • the bacterial cellulose film is applied on the skin for sebum removal. Because the bacterial cellulose film nicely fits the skin, the microbial nano-fibers of the film are able to contact with the sebum in the skin pore. When the water of the film is absorbed by the skin or volatized to dry, the sebum in the skin pore is adhesive to the film due to a siphoning effect and is removed out (see Fig. 7A and 7B ). Therefore, the bacterial cellulose film of the invention is able to remove excessive sebum not only from the surface of skin but also inside skin pores. In one embodiment, the sebum amount on the skin surface is decreased 50% ⁇ 100% after the bacterial cellulose film is applied for 15-60 minutes thereto compared to an untreated surface of skin.
  • the bacterial cellulose film of the invention is not limited in its uses and is able to be applied to any part of the surface of human or animal skin.
  • the bacterial cellulose film is applied on the surface of human or animal skin for about 15 ⁇ 60 minutes.
  • the film is applied on the surface of skin until the film became thin, dried or transparent and subsequently removed from the surface of the skin.
  • the film on the surface of skin is rinsed to remove.
  • the "rinse" in the content refers to making the bacterial cellulose film moist and softened by water, lotion or solutions in order to be easily removed from the surface of the skin.
  • Example 1 Production of the bacterial cellulose film with a density gradient in the direction of the film thickness. 10 ⁇ 30g/L of glucose and 5 ⁇ 10g/L of a yeast extract powder were used for the seed culture medium. Glyconacetobacter xylinus was implanted and cultured in this sterilized seed culture medium at 30°C and aerated for 3 ⁇ 7 days (see Fig. 2 , S1). A culture medium with 10 ⁇ 30g/L of glucose, 5 ⁇ 10g/L of a yeast extract powder, 2 ⁇ 10g/L of Na 2 HPO 4 and 1 ⁇ 5g/L of citrate acid (sterilized under 121°C for 30 minutes) were inoculated with 1 ⁇ 10% (v/v) seed cultures.
  • the initial cell number should be set in the range of 10 2 -10 5 /ml.
  • the strain was statically fermented in A4-sized plates at 25 ⁇ 28°C for 2 ⁇ 4 days. (see Fig. 2 , S2). After that, the culture temperature was increased up to 29 ⁇ 32°C for another 3 ⁇ 10days. Following fermentation, the bacterial cellulose film was moved out from the plate. Subsequently, the film was washed by 0.1% ⁇ 5% of a NaOH aqueous solution and soaked in the solution for overnight. The film was further washed with water for 3 ⁇ 4 times and then neutralized with citric acid (see Fig. 2 , S3). The obtained film was stored for the next steps.
  • the bacterial cellulose film obtained from Example 1 and a commercially available cellulose sheet were individually cut into 5 cm-diameter circles.
  • the circular films and sheet were separately immerged in a 10% glycerol aqueous solution (glycerol was one of the humectants) and applied onto the surface of a human skin for 30 minutes, in which the film surface in contact with the skin comprised the upper surface of the bacterial cellulose film in saturation with glycerol (B), the lower surface of the bacterial cellulose film in saturation with glycerol (C), the upper surface of the bacterial cellulose film in un-saturation with glycerol (D) and the surface of the commercially available cellulose sheet (E).
  • glycerol was one of the humectants
  • the test result is shown in Fig. 3 .
  • the water content of the skin surface before treatment was set as 0%. Compared to the 0%, the water loss decreased 36.1% after the surface of skin was applied the upper surface of the bacterial cellulose film in saturation with glycerol (B) for 30 minutes.
  • the treatment with the lower surface of the bacterial cellulose film in saturation with glycerol (C) also showed a negative water loss rate.
  • the result revealed that the bacterial cellulose film in a state of saturation, no mater whether the upper or lower surface was applied to the skin, was able to deliver glycerol to the skin and reduced the water loss of the skin surface.
  • the bacterial cellulose film obtained from Example 1 and a commercially available cellulose sheet (ChiaMeei Food Industrial Corp., Taichung, Taiwan) were individually cut into 5 cm-diameter circles.
  • the circular films and sheet were separately applied to a prewashed or unwashed surface of the skin of a human forehead. After about 15-40 minutes, the bacterial cellulose film was completely dried and became transparent. The commercially available cellulose sheet was still wet.
  • the circular film and sheet were separately rinsed by water and removed from the surface of skin. After 5 minutes, the treated skin surfaces were tested for the amount of sebum secretion by a CK Electronic Multiprobe Adapter System MPA580® (Custometer) (COURAGE+KHAZAKA electronic GmbH, Germany).
  • Fig. 4 shows the test result for the circular film and sheet applied to the unwashed skin surface of the human forehead. Compared to the sebum secretion before applying the film or sheet (as 100%), the treatment of the bacterial cellulose film reduced approximately 92% of the sebum from the surface of the skin, while the treatment of the commercially available sheet reduced about 30% of the sebum.
  • Fig. 5 shows the test result for the circular film and sheet applied to the prewashed surface of skin of the human forehead.
  • the treatment of the bacterial cellulose film reduced approximately 100% of the sebum secretion from the surface of the skin, while the treatment of the commercially available sheet reduced about 62% of the sebum.
  • the bacterial cellulose film obtained from Example 1 and a commercially available cellulose sheet (ChiaMeei Food Industrial Corp., Taichung, Taiwan) were individually cut into 5 cm-diameter circles and weighted (W1). Then, the circular film and sheet were dried in an oven at 50°C and weighted (W2). According to W1 and W2, the water content, water content per unit area, the weight of fibers per unit area and the amount of water per fiber were calculated according to the following formula. The result is shown in Table 1.
  • Weight of fibers per unit area (W3) W2 ⁇ 25cm 2
  • the amount of water per fiber (W1-W2) ⁇ W3 [Table 1] The water content and dry weight of the bacterial cellulose film and commercially available sheet Water content (%) Water content per unit area (g/m 2 ) Weight of fibers per unit area (g/m 2 ) The amount of water per fiber (g/g) Bacterial cellulose film in a state of saturation 97.4 ⁇ 0.4% 410.6 ⁇ 78.8 10.9 ⁇ 1.3 37.6 ⁇ 5.4 Bacterial cellulose film in a state of unsaturation 95.1 ⁇ 0.8% 232.8 ⁇ 19.5 12.1 ⁇ 2.3 19.8 ⁇ 3.3 Commercially available cellulose sheet 96.7 ⁇ 0.2% 921.2 ⁇ 49.0 31.4 ⁇ 2.9 29.4 ⁇ 1.7
  • the bacterial cellulose film was clearly different when compared to the commercially available sheet in the weight of fibers per unit area.
  • the weight of fibers per unit area for the commercially available sheet was more than 2 times than that for the bacterial cellulose film.
  • the water content per unit area and the amount of water per fiber also showed differences between the commercially available sheet and the bacterial cellulose film. The result reveals that, the bacterial cellulose film absorbs less water to reach a state of saturation. This is the reason that the bacterial cellulose film of the invention is lighter and fit better to the skin when compared with the commercially available sheet.

Landscapes

  • Organic Chemistry (AREA)
  • Chemical & Material Sciences (AREA)
  • Engineering & Computer Science (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Health & Medical Sciences (AREA)
  • Zoology (AREA)
  • Wood Science & Technology (AREA)
  • General Chemical & Material Sciences (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Bioinformatics & Cheminformatics (AREA)
  • General Health & Medical Sciences (AREA)
  • Biochemistry (AREA)
  • Biotechnology (AREA)
  • Genetics & Genomics (AREA)
  • General Engineering & Computer Science (AREA)
  • Microbiology (AREA)
  • Veterinary Medicine (AREA)
  • Animal Behavior & Ethology (AREA)
  • Dermatology (AREA)
  • Medicinal Chemistry (AREA)
  • Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
  • Public Health (AREA)
  • Pharmacology & Pharmacy (AREA)
  • Cosmetics (AREA)
  • Materials For Medical Uses (AREA)
  • Preparation Of Compounds By Using Micro-Organisms (AREA)
  • Medicinal Preparation (AREA)
EP11167341.4A 2010-05-24 2011-05-24 Film de cellulose bactérienne et sa préparation Not-in-force EP2390344B1 (fr)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
TW99116470 2010-05-24

Publications (2)

Publication Number Publication Date
EP2390344A1 true EP2390344A1 (fr) 2011-11-30
EP2390344B1 EP2390344B1 (fr) 2015-06-03

Family

ID=44454057

Family Applications (1)

Application Number Title Priority Date Filing Date
EP11167341.4A Not-in-force EP2390344B1 (fr) 2010-05-24 2011-05-24 Film de cellulose bactérienne et sa préparation

Country Status (3)

Country Link
US (1) US8772003B2 (fr)
EP (1) EP2390344B1 (fr)
TW (1) TWI408232B (fr)

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO2020223778A1 (fr) * 2019-05-06 2020-11-12 Biocelltis Biotecnologia S/A Matrice 3d de nanocellulose pour la culture de cellules humaines et animales in vitro

Families Citing this family (18)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
TW201323021A (zh) * 2011-12-12 2013-06-16 Chia Meei Food Ind Corp 生物纖維敷料及其製備方法與用途
CN103083136B (zh) * 2012-12-26 2014-06-04 东华大学 一种三明治结构的细菌纤维素液体吸收性材料及其制备方法
CN102991037B (zh) * 2012-12-26 2015-02-18 东华大学 一种三明治结构的细菌纤维素缓释载体材料及其制备方法
CN103222932B (zh) * 2013-04-22 2015-10-21 东华大学 一种激光治疗术后修复面膜及其制备方法
CN103211715B (zh) * 2013-04-22 2015-04-08 东华大学 一种具有梯度结构的细菌纤维素面膜及其制备方法
TWI586373B (zh) * 2014-02-06 2017-06-11 奈菲兒生醫股份有限公司 含有生物纖維膜碎片之化妝品組成物及其製造方法
US10682257B2 (en) * 2015-07-29 2020-06-16 Evophancie Biotech Ltd Biological fiber composite dressing
US20170028100A1 (en) * 2015-07-29 2017-02-02 Harvest Belle Biotech Biological fiber membrane and method for preparing the same
ES2955825T3 (es) 2015-11-25 2023-12-07 JeNaCell GmbH Artículo que contiene celulosa producido biotecnológicamente para uso dermatológico
CN105754125B (zh) * 2016-03-02 2017-07-04 山东纳美德生物科技有限公司 一种细菌纤维素干膜及其制备方法、应用
US11180627B2 (en) 2017-01-11 2021-11-23 The Regents Of The University Of Colorado, A Body Corporate Cellulose enabled orientationally ordered flexible gels
CN107281000A (zh) * 2017-06-23 2017-10-24 南京理工大学 一种细菌纤维素面膜的使用方法
JP6694856B2 (ja) * 2017-07-25 2020-05-20 王子ホールディングス株式会社 繊維状セルロース含有組成物、その製造方法、及び膜
CN108395563B (zh) * 2018-05-30 2021-03-09 陕西科技大学 一种细菌纤维素粉末的制备方法
AU2019287564B2 (en) * 2018-06-13 2024-05-23 The Regents Of The University Of Colorado, A Body Corporate Bacterial cellulose gels, process for producing and methods of use
KR20200035899A (ko) * 2018-09-27 2020-04-06 주식회사 엘지화학 바이오셀룰로오스 시트 및 이의 제조 방법
CN114159981B (zh) * 2021-11-20 2023-08-22 宁波大学 一种功能化纤维素改性疏水型高分子微滤膜的方法
WO2023242352A1 (fr) * 2022-06-17 2023-12-21 Consejo Superior De Investigaciones Científicas (Csic) Articles à base de gels de cellulose présentant des propriétés de barrière améliorées

Citations (19)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO1986002095A1 (fr) 1984-10-01 1986-04-10 Bio Fill Industria E Comercio De Produtos Medico H Procede de preparation d'un film a base de cellulose, film a base de cellulose produit par ce procede, greffe de peau artificielle, et son utilisation
US4588400A (en) 1982-12-16 1986-05-13 Johnson & Johnson Products, Inc. Liquid loaded pad for medical applications
EP0396344A2 (fr) 1989-04-28 1990-11-07 Ajinomoto Co., Inc. Cellulose microbienne creuse, procédé de préparation et vaisseau sanguin artificiel formé à partir de cette cellulose
EP0457474A2 (fr) 1990-05-18 1991-11-21 Sony Corporation Procédé de fabrication d'une membane acoustique
US5274199A (en) 1990-05-18 1993-12-28 Sony Corporation Acoustic diaphragm and method for producing same
JPH06284495A (ja) 1993-01-29 1994-10-07 Sony Corp 音響振動板及びその製造方法
JPH1077302A (ja) 1996-08-30 1998-03-24 Bio Polymer Res:Kk バクテリアセルロースの可溶化物
WO2001061026A1 (fr) 2000-02-17 2001-08-23 Sura Chemicals Gmbh Procede et dispositif de production de cellulose microbienne moulee destinee a servir de biomateriau, notamment pour la microchirurgie
EP1438975A1 (fr) 2003-01-16 2004-07-21 Xylos Corporation Pansement à base d'un gel amorphé contenant un dérivé microbien de la cellulose
US20050019380A1 (en) 2002-04-26 2005-01-27 Xylos Corporation Microbial cellulose wound dressing for treating chronic wounds
WO2005018435A2 (fr) 2003-08-22 2005-03-03 Xylos Corporation Cellulose derivee de microbes modifiee thermiquement pour implantation in vivo
EP1849463A2 (fr) 2006-04-19 2007-10-31 Xylos Corporation Matières cellulosiques microbiennes pouvant être utilisées dans des systèmes d'administration de médicaments transdermiques, procédés de fabrication et utilisation
US20070286884A1 (en) 2006-06-13 2007-12-13 Xylos Corporation Implantable microbial cellulose materials for hard tissue repair and regeneration
US20080220333A1 (en) 2004-08-30 2008-09-11 Shoichiro Yano Lithium Ion Conductive Material Utilizing Bacterial Cellulose Organogel, Lithium Ion Battery Utilizing the Same and Bacterial Cellulose Aerogel
FR2916948A1 (fr) 2007-06-06 2008-12-12 Oreal Article et dispositif pour diffuser un parfum.
FR2916971A1 (fr) 2007-06-06 2008-12-12 Oreal Ensemble amincissant.
JP2009051829A (ja) 2007-07-02 2009-03-12 L'oreal Sa 生体セルロースを含有する基体、及び該基体と接触することとなる粉末状化粧料組成物を含むアセンブリー
FR2924340A1 (fr) 2007-12-03 2009-06-05 Oreal Procede de maquillage des ongles.
FR2924342A1 (fr) 2007-12-03 2009-06-05 Oreal Produit de maquillage et/ou de soin.

Family Cites Families (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN101314788A (zh) * 2008-07-11 2008-12-03 天津实发中科百奥工业生物技术有限公司 细菌纤维素高产菌株培育筛选的方法
CN101365264A (zh) * 2008-08-22 2009-02-11 许春元 细菌纤维素音响振膜

Patent Citations (19)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US4588400A (en) 1982-12-16 1986-05-13 Johnson & Johnson Products, Inc. Liquid loaded pad for medical applications
WO1986002095A1 (fr) 1984-10-01 1986-04-10 Bio Fill Industria E Comercio De Produtos Medico H Procede de preparation d'un film a base de cellulose, film a base de cellulose produit par ce procede, greffe de peau artificielle, et son utilisation
EP0396344A2 (fr) 1989-04-28 1990-11-07 Ajinomoto Co., Inc. Cellulose microbienne creuse, procédé de préparation et vaisseau sanguin artificiel formé à partir de cette cellulose
EP0457474A2 (fr) 1990-05-18 1991-11-21 Sony Corporation Procédé de fabrication d'une membane acoustique
US5274199A (en) 1990-05-18 1993-12-28 Sony Corporation Acoustic diaphragm and method for producing same
JPH06284495A (ja) 1993-01-29 1994-10-07 Sony Corp 音響振動板及びその製造方法
JPH1077302A (ja) 1996-08-30 1998-03-24 Bio Polymer Res:Kk バクテリアセルロースの可溶化物
WO2001061026A1 (fr) 2000-02-17 2001-08-23 Sura Chemicals Gmbh Procede et dispositif de production de cellulose microbienne moulee destinee a servir de biomateriau, notamment pour la microchirurgie
US20050019380A1 (en) 2002-04-26 2005-01-27 Xylos Corporation Microbial cellulose wound dressing for treating chronic wounds
EP1438975A1 (fr) 2003-01-16 2004-07-21 Xylos Corporation Pansement à base d'un gel amorphé contenant un dérivé microbien de la cellulose
WO2005018435A2 (fr) 2003-08-22 2005-03-03 Xylos Corporation Cellulose derivee de microbes modifiee thermiquement pour implantation in vivo
US20080220333A1 (en) 2004-08-30 2008-09-11 Shoichiro Yano Lithium Ion Conductive Material Utilizing Bacterial Cellulose Organogel, Lithium Ion Battery Utilizing the Same and Bacterial Cellulose Aerogel
EP1849463A2 (fr) 2006-04-19 2007-10-31 Xylos Corporation Matières cellulosiques microbiennes pouvant être utilisées dans des systèmes d'administration de médicaments transdermiques, procédés de fabrication et utilisation
US20070286884A1 (en) 2006-06-13 2007-12-13 Xylos Corporation Implantable microbial cellulose materials for hard tissue repair and regeneration
FR2916948A1 (fr) 2007-06-06 2008-12-12 Oreal Article et dispositif pour diffuser un parfum.
FR2916971A1 (fr) 2007-06-06 2008-12-12 Oreal Ensemble amincissant.
JP2009051829A (ja) 2007-07-02 2009-03-12 L'oreal Sa 生体セルロースを含有する基体、及び該基体と接触することとなる粉末状化粧料組成物を含むアセンブリー
FR2924340A1 (fr) 2007-12-03 2009-06-05 Oreal Procede de maquillage des ongles.
FR2924342A1 (fr) 2007-12-03 2009-06-05 Oreal Produit de maquillage et/ou de soin.

Non-Patent Citations (4)

* Cited by examiner, † Cited by third party
Title
BODIN ET AL: "Influence of cultivation conditions on mechanical and morphological properties of bacterial cellulose tubes", BIOTECHNOLOGY AND BIOENGINEERING, vol. 97, 2007, pages 425 - 434, XP002446749 *
MENDES ET AL: "In vivo and in vitro evaluation of an Acetobacter xylinum synthesized microbial cellulose membrane intended for guided tissue repair", ACTA VETERINARIA SCANDINAVICA, vol. 51, 2009, pages 1 - 8, XP021052382 *
N.N.: "Hydro-Velour", COSMOPROF ASIA 2009, 2009, pages 1, XP002657363, Retrieved from the Internet <URL:www.hydro-velour.com/news-ndetail-1-2.html> [retrieved on 20110823] *
TANG ET AL: "The influence of fermentation conditions and post-treatment methods on porosity of bacterial cellulose membrane", WORLD JOURNAL OF MICROBIOLOGY AND BIOTECHNOLOGY, vol. 26, 20 August 2009 (2009-08-20), pages 125 - 131, XP019775541 *

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO2020223778A1 (fr) * 2019-05-06 2020-11-12 Biocelltis Biotecnologia S/A Matrice 3d de nanocellulose pour la culture de cellules humaines et animales in vitro

Also Published As

Publication number Publication date
TWI408232B (zh) 2013-09-11
US20110286948A1 (en) 2011-11-24
TW201142033A (en) 2011-12-01
US8772003B2 (en) 2014-07-08
EP2390344B1 (fr) 2015-06-03

Similar Documents

Publication Publication Date Title
EP2390344B1 (fr) Film de cellulose bactérienne et sa préparation
US8951551B2 (en) Multiribbon nanocellulose as a matrix for wound healing
CN103211715B (zh) 一种具有梯度结构的细菌纤维素面膜及其制备方法
WO2015085633A1 (fr) Hydrogel à base de polymère réticulé d&#39;acide γ-polyglutamique et de ε-polylysine, et son procédé de préparation
US20180216148A1 (en) Composite cellulose hydrogels and methods of making and use thereof
CN102212208A (zh) 细菌纤维素/透明质酸复合材料的制备方法
CN114072128B (zh) 具有皮肤保湿以及皮肤再生功能的皮肤益生菌块组合物的制造方法
CN108635249B (zh) 一种水凝胶基底面膜组合物及其制备方法
KR101805171B1 (ko) 바이오 셀룰로오스 페이퍼 및 이의 제조방법
Foresti et al. Bacterial nanocellulose: Synthesis, properties and applications
CN103083112B (zh) 一种具备疏密结构的细菌纤维素皮肤修复材料及其制备方法
CN106265474B (zh) 一种利用微生物菌株发酵生产面膜的方法
CN103222932B (zh) 一种激光治疗术后修复面膜及其制备方法
US20210140100A1 (en) Bio-cellulose sheet and preparation method thereof
WO2014133249A1 (fr) Procédé de préparation de gel cellulosique microbien
WO2012003640A1 (fr) Membrane de fibres biologiques et son utilisation
CN106214499A (zh) 一种面膜基材的制备方法
KR20180119282A (ko) 고체 원물이 포함된 바이오셀룰로오스, 이를 제조하기 위한 배지 조성물 및 이의 제조방법
KR102084943B1 (ko) 숙성 프로폴리스를 함유한 바이오셀룰로오스 마스크 팩 및 그 제조방법
KR101802930B1 (ko) 글루코노박터 우치무레 GFC-cellul15 균주 및 이로부터 제조된 바이오셀룰로오스
CN112791100A (zh) 一种兼具高效活性氧清除功能的复合抗菌微球及其制备方法
BODEA et al. Bacterial biofilms as wound healing dressing-a review.
CN112826983A (zh) 一种心脏脱细胞基质修饰仿生膜及其制备和应用
KR101875527B1 (ko) 건조 바이오셀룰로오스 시트의 제조방법 및 이로부터 제조된 건조 바이오셀룰로오스 시트
CN113197813A (zh) 一种蚕丝蛋白-纤维素纳米复合面膜的制备方法

Legal Events

Date Code Title Description
AK Designated contracting states

Kind code of ref document: A1

Designated state(s): AL AT BE BG CH CY CZ DE DK EE ES FI FR GB GR HR HU IE IS IT LI LT LU LV MC MK MT NL NO PL PT RO RS SE SI SK SM TR

AX Request for extension of the european patent

Extension state: BA ME

PUAI Public reference made under article 153(3) epc to a published international application that has entered the european phase

Free format text: ORIGINAL CODE: 0009012

17P Request for examination filed

Effective date: 20120321

17Q First examination report despatched

Effective date: 20120726

GRAP Despatch of communication of intention to grant a patent

Free format text: ORIGINAL CODE: EPIDOSNIGR1

INTG Intention to grant announced

Effective date: 20141028

GRAS Grant fee paid

Free format text: ORIGINAL CODE: EPIDOSNIGR3

RIN1 Information on inventor provided before grant (corrected)

Inventor name: WEY, YUH-CHYUN

Inventor name: LIN, YI-CHUAN

Inventor name: LEE, MEI-LING

RAP1 Party data changed (applicant data changed or rights of an application transferred)

Owner name: NYMPHEAS INTERNATIONAL CORPORATION

GRAA (expected) grant

Free format text: ORIGINAL CODE: 0009210

RAP1 Party data changed (applicant data changed or rights of an application transferred)

Owner name: NYMPHEAS INTERNATIONAL CORPORATION

AK Designated contracting states

Kind code of ref document: B1

Designated state(s): AL AT BE BG CH CY CZ DE DK EE ES FI FR GB GR HR HU IE IS IT LI LT LU LV MC MK MT NL NO PL PT RO RS SE SI SK SM TR

REG Reference to a national code

Ref country code: GB

Ref legal event code: FG4D

REG Reference to a national code

Ref country code: CH

Ref legal event code: EP

REG Reference to a national code

Ref country code: AT

Ref legal event code: REF

Ref document number: 729959

Country of ref document: AT

Kind code of ref document: T

Effective date: 20150715

Ref country code: IE

Ref legal event code: FG4D

REG Reference to a national code

Ref country code: DE

Ref legal event code: R096

Ref document number: 602011016878

Country of ref document: DE

REG Reference to a national code

Ref country code: AT

Ref legal event code: MK05

Ref document number: 729959

Country of ref document: AT

Kind code of ref document: T

Effective date: 20150603

PG25 Lapsed in a contracting state [announced via postgrant information from national office to epo]

Ref country code: NO

Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT

Effective date: 20150903

Ref country code: ES

Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT

Effective date: 20150603

Ref country code: HR

Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT

Effective date: 20150603

Ref country code: LT

Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT

Effective date: 20150603

Ref country code: FI

Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT

Effective date: 20150603

REG Reference to a national code

Ref country code: NL

Ref legal event code: MP

Effective date: 20150603

REG Reference to a national code

Ref country code: LT

Ref legal event code: MG4D

PG25 Lapsed in a contracting state [announced via postgrant information from national office to epo]

Ref country code: LV

Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT

Effective date: 20150603

Ref country code: RS

Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT

Effective date: 20150603

Ref country code: GR

Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT

Effective date: 20150904

Ref country code: AT

Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT

Effective date: 20150603

Ref country code: BG

Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT

Effective date: 20150903

PG25 Lapsed in a contracting state [announced via postgrant information from national office to epo]

Ref country code: EE

Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT

Effective date: 20150603

PG25 Lapsed in a contracting state [announced via postgrant information from national office to epo]

Ref country code: SK

Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT

Effective date: 20150603

Ref country code: PL

Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT

Effective date: 20150603

Ref country code: PT

Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT

Effective date: 20151006

Ref country code: IS

Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT

Effective date: 20151003

Ref country code: CZ

Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT

Effective date: 20150603

Ref country code: RO

Free format text: LAPSE BECAUSE OF NON-PAYMENT OF DUE FEES

Effective date: 20150603

REG Reference to a national code

Ref country code: DE

Ref legal event code: R097

Ref document number: 602011016878

Country of ref document: DE

PLBE No opposition filed within time limit

Free format text: ORIGINAL CODE: 0009261

STAA Information on the status of an ep patent application or granted ep patent

Free format text: STATUS: NO OPPOSITION FILED WITHIN TIME LIMIT

PG25 Lapsed in a contracting state [announced via postgrant information from national office to epo]

Ref country code: IT

Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT

Effective date: 20150603

Ref country code: DK

Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT

Effective date: 20150603

26N No opposition filed

Effective date: 20160304

REG Reference to a national code

Ref country code: FR

Ref legal event code: PLFP

Year of fee payment: 6

PG25 Lapsed in a contracting state [announced via postgrant information from national office to epo]

Ref country code: SI

Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT

Effective date: 20150603

PG25 Lapsed in a contracting state [announced via postgrant information from national office to epo]

Ref country code: BE

Free format text: LAPSE BECAUSE OF NON-PAYMENT OF DUE FEES

Effective date: 20160531

PG25 Lapsed in a contracting state [announced via postgrant information from national office to epo]

Ref country code: LU

Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT

Effective date: 20160524

Ref country code: BE

Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT

Effective date: 20150603

REG Reference to a national code

Ref country code: CH

Ref legal event code: PL

GBPC Gb: european patent ceased through non-payment of renewal fee

Effective date: 20160524

PG25 Lapsed in a contracting state [announced via postgrant information from national office to epo]

Ref country code: LI

Free format text: LAPSE BECAUSE OF NON-PAYMENT OF DUE FEES

Effective date: 20160531

Ref country code: CH

Free format text: LAPSE BECAUSE OF NON-PAYMENT OF DUE FEES

Effective date: 20160531

REG Reference to a national code

Ref country code: IE

Ref legal event code: MM4A

REG Reference to a national code

Ref country code: FR

Ref legal event code: PLFP

Year of fee payment: 7

PG25 Lapsed in a contracting state [announced via postgrant information from national office to epo]

Ref country code: GB

Free format text: LAPSE BECAUSE OF NON-PAYMENT OF DUE FEES

Effective date: 20160524

Ref country code: IE

Free format text: LAPSE BECAUSE OF NON-PAYMENT OF DUE FEES

Effective date: 20160524

PG25 Lapsed in a contracting state [announced via postgrant information from national office to epo]

Ref country code: NL

Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT

Effective date: 20150603

Ref country code: SE

Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT

Effective date: 20150603

PG25 Lapsed in a contracting state [announced via postgrant information from national office to epo]

Ref country code: CY

Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT

Effective date: 20150603

Ref country code: HU

Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT; INVALID AB INITIO

Effective date: 20110524

Ref country code: SM

Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT

Effective date: 20150603

REG Reference to a national code

Ref country code: FR

Ref legal event code: PLFP

Year of fee payment: 8

PG25 Lapsed in a contracting state [announced via postgrant information from national office to epo]

Ref country code: MK

Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT

Effective date: 20150603

Ref country code: TR

Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT

Effective date: 20150603

Ref country code: MC

Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT

Effective date: 20150603

Ref country code: MT

Free format text: LAPSE BECAUSE OF NON-PAYMENT OF DUE FEES

Effective date: 20160531

PGFP Annual fee paid to national office [announced via postgrant information from national office to epo]

Ref country code: FR

Payment date: 20180531

Year of fee payment: 8

PG25 Lapsed in a contracting state [announced via postgrant information from national office to epo]

Ref country code: AL

Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT

Effective date: 20150603

PGFP Annual fee paid to national office [announced via postgrant information from national office to epo]

Ref country code: DE

Payment date: 20180731

Year of fee payment: 8

REG Reference to a national code

Ref country code: DE

Ref legal event code: R119

Ref document number: 602011016878

Country of ref document: DE

PG25 Lapsed in a contracting state [announced via postgrant information from national office to epo]

Ref country code: DE

Free format text: LAPSE BECAUSE OF NON-PAYMENT OF DUE FEES

Effective date: 20191203

PG25 Lapsed in a contracting state [announced via postgrant information from national office to epo]

Ref country code: FR

Free format text: LAPSE BECAUSE OF NON-PAYMENT OF DUE FEES

Effective date: 20190531